Monika Andrassi-Darida

Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype–phenotype correlation

Christina Gerth‐Kahlert, Monika Andrassi-Darida, Markus Böck et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2002 · 86 citations

Ocular Disease, Ophthalmology, Genetics +8

RETINAL VASCULAR DEVELOPMENT WITH 0.312 MG INTRAVITREAL BEVACIZUMAB TO TREAT SEVERE POSTERIOR RETINOPATHY OF PREMATURITY

Birgit Lorenz, Knut Stieger, Melanie Jäger et al. · Retina · 2016 · 81 citations · Full text

OCT-Based Macular Structure–Function Correlation in Dependence on Birth Weight and Gestational Age—the Giessen Long-Term ROP Study

Wadim Bowl, Knut Stieger, Magdalena Bokun et al. · Investigative Ophthalmology & Visual Science · 2016 · 73 citations · Full text

OCT Angiography in Young Children with a History of Retinopathy of Prematurity

Wadim Bowl, Marianne Bowl, Silke Schweinfurth et al. · Ophthalmology Retina · 2018 · 46 citations

Ocular Disease, Ophthalmology, Oct Angiography +6

Large deletions of the<i>KCNV2</i>gene are common in patients with cone dystrophy with supernormal rod response

Bernd Wissinger, Simone Schaich, Britta Baumann et al. · Human Mutation · 2011 · 41 citations · Full text

Channelopathies, Ocular Disease, Retina +12